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Journal of Animal Health and Production

JAHP_7_1_32-37

 

 

Research Article

 

Prevalence and Antibiotic Susceptibility Pattern of Staphylococcus aureus, Streptococcus agalactiae and Escherichia coli in Dairy Goats with Clinical and Subclinical Mastitis

 

Siti Mariam Zainal Ariffin*, Nurhasnida Hasmadi, Nadhirah Mohamed Syawari, Muhammad Zikree Sukiman, Muhammad Faiq Tajol Ariffin, Chai Min Hian, Mohd Faizal Ghazali

School of Animal Science, Faculty of Bioresources and Food Industry, Universiti Sultan Zainal Abidin (UniSZA), Besut Campus, 22200, Besut, Terengganu, Malaysia.

 

Abstract | Mastitis is a common disease in lactating goats that widespread throughout the world. This study aims to determine the prevalence of Staphylococcus aureus (S. aureus), Streptococcus agalactiae (S. agalactiae) and Escherichia coli (E. coli) in clinical and subclinical mastitis in does, and to identify the antibiotic susceptibility of the isolated bacteria. A total of 145 milk samples were collected from different farms located around Besut and Setiu districts, Terengganu, Peninsular Malaysia. All does were screened for subclinical mastitis using the California Mastitis Test. Signs of clinical mastitis were recorded. The milk samples were inoculated on Mannitol salt agar, blood agar and Eosin-Methylene Blue agar. The isolated bacterial colonies were subjected to Gram’s staining and biochemical tests (catalase, coagulase, oxidase, triple sugar iron and Christie, Atkins, and Munch-Peterson tests) for identification. The susceptibility of S. aureus, S. agalactiae, and E. coli to the antibiotic was tested using disc diffusion assay. The prevalence of clinical and subclinical mastitis was 23% (34/145) and 40% (58/145) respectively. The bacteriological examinations revealed that 15/92 (16.3%), 6/92 (6.5%) and 1/92 (1.1%) of the mastitis samples were positive for S. aureus, S. agalactiae, and E. coli respectively. Overall resistance levels were very low except for S. aureus towards penicillin (22%) and tetracycline (11%) and for S. agalactiae towards penicillin (33.3%). In conclusion, S. aureus was the most frequently isolated organisms from the caprine mastitis followed by S. agalactiae and E. coli in the study area.

 

Keywords | Mastitis, Goats, S. aureus, S. agalactiae, E. coli, Antibiotic susceptibility

 

Editor | Asghar Ali Kamboh, Sindh Agriculture University, Tandojam, Pakistan.

Received | December 31, 2018; Accepted | February 18, 2019; Published | February 28, 2019

*Correspondence | Siti Mariam Zainal Ariffin, School of Animal Science, Faculty of Bioresources and Food Industry, Universiti Sultan Zainal Abidin (UniSZA), Besut Campus, 22200, Besut, Terengganu, Malaysia; Email: sitimariam@unisza.edu.my

Citation | Ariffin SMZ, Hasmadi N, Syawari NM, Sukiman MZ, Faiq TAM, Chai MH, Ghazali MF (2019). Prevalence and antibiotic susceptibility pattern of Staphylococcus aureus, Streptococcus agalactiae and Escherichia coli in dairy goats with clinical and subclinical mastitis . J. Anim. Health Prod. 7(1): 32-37.

DOI | http://dx.doi.org/10.17582/journal.jahp/2019/7.1.32.37

ISSN | 2308-2801

Copyright © 2019 Ariffin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

 

INTRODUCTION

 

Mastitis is an inflammation of the parenchyma of the mammary gland. This condition is a major endemic disease that can affect all lactating animals (Rinaldi et al., 2010). It is a particular concern for farmers and veterinarian in developing countries like Malaysia. Depending on the severity of the disease, mastitis causes the majority of economic losses to the dairy producers. Costs associated with mastitis include reduced milk production and quality, increased veterinary cost, increased risk of culling of infected animals and deaths (Seegers et al., 2003).

 

Mastitis can be classified as clinical or subclinical. Dairy goats with clinical mastitis usually show signs of inflammation such as redness, heat, pain and swollen udders (Sarker and Samad, 2011). Visible abnormalities in the milk like clots, flakes, abnormal colour and blood are also common (Dasohari and Kandula, 2017). Goats with subclinical mastitis do not show apparent signs and commonly detected by elevation of somatic cell count (SCC) or by California Mastitis Test (CMT). Mastitis is caused by various pathogens as either contagious or environmental. The most frequently isolated pathogens include Staphylococcus spp., Streptococcus spp., E. coli, and Pasteurella spp. (Contreras et al., 2007).

 

Antimicrobial therapy is used to treat mastitis in small ruminants along with antibiotic susceptibility testing to ensure optimum therapeutic action (Landfried et al., 2018). The emergence of multidrug-resistant bacteria has become a major threat to animal and human health (Parra et al., 2017). This problem may not only limit the option for effective treatment but also spreading of the resistance genes from contaminated milk to human normal flora (Hameed et al., 2007).

 

In major part of Malaysia, the disease is insufficiently investigated and published information regarding to its magnitude and causative agents among small ruminant is scant. Therefore the present study aimed to determine the prevalence and major bacterial causes of mastitis in goats. The antibiotic susceptibility pattern of the isolated bacteria were also investigated.

 

MATERIALS AND METHODS

 

Sample Collection

A total of 145 raw milk samples were collected from two districts (Besut and Setiu) of Terengganu, Peninsular Malaysia during January to May 2018. Prior to sampling, all lactating animals were screened and scored for mastitis using the California Mastitis Test (CMT) according to the method described by Lucia et al. (2017). Any signs of clinical mastitis such as swelling, heat, hardness, redness, or pain of the udder were recorded. Approximately, 6 ml of mid-stream milk was collected from both udders. The milk was aseptically collected by hand-stripping and stored in a sterile polystyrene tube. After collection, samples were placed in the icebox and transported to the Microbiology Laboratory, Faculty of Bioresources and Food Industry, Universiti Sultan Zainal Abidin, Besut Campus for further processing and microbiological analysis.

 

Bacteriological Culture and Identification

Milk samples were plated on Mannitol salt agar (MSA), 5% goat blood agar and Eosin-Methylene Blue agar. The inoculated plates were incubated at 37˚C for about 24 to 48 hours. Colonies suspected of being S. aureus, S. agalactiae and E. coli were initially identified by their colony morphology, Gram’s staining and conventional biochemical tests (catalase, coagulase, oxidase, triple sugar iron (TSI) and Christie, Atkins, and Munch-Peterson (CAMP) tests) as per the method of Quinn et al. (2004).

 

Antibiotic Susceptibility Testing

The Kirby-Bauer disc diffusion method was used to determine the antibiotic susceptibility of isolates. A single colony from the fresh culture was picked with a sterile loop and suspended into Mueller Hinton Broth (MHB). The broth was then left at room temperature for 30 minutes. The densities of the bacterial suspensions were adjusted equal to the 0.5 McFarland standards. 10 µl from each isolate suspension was cultured on Mueller Hinton agar by sterile cotton swab. The susceptibility profiles of isolates towards different types of antibiotics are listed in Table 3 as suggested by Hinthong et al. (2017), Magiorakos et al. (2012) and Tomazi et al. (2018). The plates were incubated at 37 ºC for 18 to 24 hours. The breakpoints of Clinical Laboratory Standard Institute (CLSI) for the tested antibiotics were used to determine the susceptibility profiles. E. coli ATCC 25922 and S. aureus ATCC 25923 were included as positive controls in each assay.

 

Statistical Analysis

The data generated from this experiment were organized in Microsoft Excel (2010) worksheet for further descriptive analyses. The prevalence (%) of S. aureus, S. agalactiae and E. coli mastitis was calculated by dividing the number of cases by the total number of the affected animals. One-way ANOVA was performed using GraphPad Prism for Windows, version 7 (GraphPad Software Incorporation, California, USA) to compare S. aureus, S. agalactiae and E. coli intramammary infection between the studied area and to compare between mastitis status.

 

RESULTS

 

Prevalence of S. aureus, S. agalactiae and E. coli in Dairy Goats with Clinical and Subclinical Mastitis

The findings of the CMT and clinical examination confirmed overall 63.4% prevalence of caprine mastitis in the study areas. Out of the 145 milk samples, 34 (23%) were clinical mastitis and 58 (40%) were subclinical mastitis respectively (Table 1). Our findings showed that the prevalence of mastitis varied with the categories of mastitis and the study area and the difference was significantly difference (P<0.05) (Figure 1). The bacteriological examinations revealed that 31/92 (33.7%), 6/92 (6.5%) and 1/92 (1.1%) of the mastitic samples were positive for S. aureus, S. agalactiae and E. coli (Table 2). There was no significant difference in finding bacteriologically positive samples between subclinical mastitis (n=58, 41.4%) and clinical mastitis (n=34, 41.2%) (P>0.05).

 

Table 1: Number and type of samples collected from goat mastitis.

 

Study area Clinical mastitis Subclinical mastitis Total samples
Besut 3 19 22
Setiu 31 39 70
Total 34 58 92

 

Table 2: Prevalence of S. aureus, S. agalactiae and E. coli in goat mastitis in Besut and Setiu, Terengganu, Malaysia.

 

Besut, Terengganu

Types of samples No. of samples S. aureus S. agalactiae E. coli Total isolates
No % No % No % No %
Clinical mastitis 3 0 0 1 33.0 0 0 1 33.3
Subclinical mastitis 19 8 44.4 0 0 0 0 8 44.4
Total 22 8 36.4 1 4.5 0 0 9 41.0
Setiu, Terengganu

Types of samples No. of samples S. aureus S. agalactiae E. coli Total isolates
No % No % No % No %
Clinical mastitis 31 12 38.7 2 6.4 0 0 14 45.2
Subclinical mastitis 39 11 28.2 3 7.7 1 2.6 15 38.5
Total 70 23 32.8 5 7.1 1 1.4 29

41.4

 

Table 3: Overall antibiotic susceptibility pattern of S. aureus, S. agalactiae and E.coli isolated from clinical and subclinical mastitis in goats.

 

  Number of isolates (%)
Isolates Antimicrobials Symbol Disk Potency (µg) Resistant Intermediate Sensitive
S. aureus Penicillin P 10 2 (6.45) 0 (0) 29 (93.55)
Gentamicin CN 10 0 (0) 0 (0) 31 (100)
Nitrofurantoin F 300 0 (0) 0 (0) 31 (100)
Oxacillin OX 1 0 (0) 0 (0) 31 (100)
Cefoxitin FOX 30 0 (0) 0 (0) 31 (100)
Norfloxacin NOR 10 0 (0) 0 (0) 31 (100)
Tetracycline TE 30 2 (6.45) 0 (0) 29 (93.55)
Amikacin AK 30 0 (0) 0 (0) 31 (100)
Kanamycin K 30 0 (0) 0 (0) 31 (100)
Doxycycline DO 5 0 (0) 0 (0) 31 (100)
Cefotaxime CTX 30 0 (0) 0 (0) 31 (100)
Amoxicillin AMC 30 0 (0) 0 (0) 31 (100)
Chloramphenicol C 30 0 (0) 0 (0)

31 (100)

S. agalactiae Vancomycin VA 30 0 (0) 0 (0) 6 (100)
Tetracycline TE 30 0 (0) 0 (0) 6 (100)
Clindamycin DA 2 0 (0) 0 (0) 6 (100)
Chloramphenicol C 30 0 (0) 0 (0) 6 (100)
Penicillin P 10 2 (33.33) 0 (0) 4 (66.67)
E. coli Chloramphenicol C 30 0 (0) 0 (0) 1 (100)
Gentamicin CN 10 0 (0) 0 (0) 1 (100)
Imipenem IPM 10 0 (0) 0 (0) 1 (100)
Norfloxacin NOR 10 0 (0) 0 (0) 1 (100)
Meropenem MEM 10 0 (0) 0 (0)

1 (100)

 

Antibiotic Susceptibility Test

Antibiotic susceptibility pattern of the isolated S. aureus, S. agalactiae and E. coli is shown in Table 3. Different level of susceptibility and resistance against some antibiotics was observed. Of the 31 isolates of S. aureus, 87% (27/31) showed full susceptibility to amoxicillin, gentamicin, nitrofurantoin, oxacillin, cefoxitin, norfloxacin, chloramphenicol, amikacin, kanamycin, doxycycline and cefotaxime. However, 6.45% (2/31) were resistant to penicillin and 6.45% (2/31) were resistant to tetracycline respectively. All of the penicillin and tetracycline-resistant isolates were from clinical mastitis.Of a total of 6 isolates of S. agalactiae, 66.7% (4/6) showed full susceptibility to vancomycin, tetracycline and clindamycin. However, 33.3% (2/6) of S. agalactiae isolates isolated from clinical mastitis were resistant to penicillin. All of the E. coli isolates revealed full susceptibility to chloramphenicol, gentamicin, imipenem, norfloxacin and meropenem.

 

 

DISCUSSION

 

Mastitis is one of the important disease in goats that threaten public health and dairy industry worldwide. Diagnosis of clinical mastitis is straightforward, based on the appearance of the mammary gland and abnormality of the milk. In contrast, subclinical mastitis, which is a hidden form of intra-mammary infection is more problematic in term of diagnosis since the milk and udder appear normal. Diagnosis of subclinical mastitis routinely rely on direct measurement of the somatic cell count level or performing a CMT. In the present study, the prevalence of clinical and subclinical mastitis was 23% and 40% respectively. This result is in contrast with that of Abdalhamed et al. (2018) who recorded 7% and 11% prevalence rates of clinical and subclinical mastitis in goats based on the results of CMT. Previous study by Ebrahimi et al. (2007) reported mastitis was found in goats only with low prevalence (5.25%). However, higher mastitis prevalence (53.5%) in dairy goat was documented by Ali et al. (2010). The difference in the prevalence rates may be attributed to a difference in the study design, study area, geographical location, management system and time.

 

In the present study, the highest percent bacteria revealed were S. aureus (34%) followed by S. agalactiae (6.5%) and E. coli (1.1%). The lower isolation rate of S. aureus is contrary to the previous studies reported from Pakistan (Najeeb et al. 2013). The rate of S. aureus was stated as 61.6%, mainly isolated from subclinical mastitis cases in dairy goat. The prevalence of S. aureus mastitis in goat that has been reported by the other studies in Malaysia (20%) (Faiq et al., 2017) and China (15%) (Zhao et al., 2015) were considerably lower than the prevalence reported in this study. According to Rahman et al. (2016), different climatic conditions, herd management and diversity of breeds may explain the differences in the prevalence of S. aureus mastitis between studied areas. S. aureus can spread during manual contact of mammary gland by the herdsman, contaminated bedding material from infected does and lambs sucking does other than their dam (Rainard et al., 2018).

 

Caprine mastitis caused by E. coli can range from being a subclinical infection of the mammary gland to a severe systemic infection. In the current study, E. coli was detected in 1/58 (1.7%) subclinical cases. This result is in agreement with that reported by White and Hinckley (1999). Jeph (2012) reported that E. coli (19%) was the main aetiological agent responsible for clinical mastitis in goats. In another study by Pirzada et al. (2016) showed that the prevalence of E. coli mastitis was 5.26%. Recently, in Bangladesh, E. coli were isolated from 27.6% of clinical mastitis cases in doe (Rudra and Dutta, 2018). E. coli mastitis is mainly attributed to environmental factors such as low levels of hygiene, contaminated litter, milking and post-milking areas pollution may increase the likelihood of invading and colonization of the pathogens. Thus, low prevalence of E. coli mastitis seen in this study might be due to improvements in herd environmental management in the study areas.

 

Mastitis caused by S. agalactiae is often reported in dairy goats. In this study, 6/92 (6.5%) mastitis samples were positive for S. agalactiae. The low prevalence of S. agalactiae was comparable with the findings of previous studies (Pirzada et al., 2016; Wakwoya et al., 2006). According to Hawari et al. (2014), the prevalence of S. agalactiae mastitis can be increased as high as 30%. S. agalactiae mastitis is a highly contagious bacterial infection that can be easily transmitted from one animal to other lactating animals (Barkema et al., 2009).

 

Mastitis pathogens have been showed to change over time, therefore bacteriological monitoring need to be regularly executed at the herd level. Microbial culture is considered most reliable and economical method to identify the disease-causing pathogens. The gold standard for identifying intramammary infections is to perform a bacteriological milk culture, with identification of the pathogen and sensitivity testing. The purpose of antimicrobial susceptibility test is to determine which specific antibiotics a particular bacteria is sensitive or resistant to, thus helping in the choice of drug to be used for treatment.

 

The antibiotic susceptibility pattern of S. aureus reported by Shamila-Syuhada et al. (2016) is in agreement with the current study where 22% isolates showed resistant to penicillin. Our results are also in line with the work by Seyoum et al. (2018) who reported that S. aureus from mastitis milk has low tetracycline resistance rates (14.2%). Multiple drug resistance (MDR) among bacteria is a worldwide problem. The emergence of MDR is due to indiscriminate and prolonged use of antimicrobial agents (Wegener, 2012). Moreover, drinking mastitis infected milk may increase risk of transmitting antibiotic resistance genes to gut microbiota of human beings (Najeeb et al., 2013). S. aureus is remarkable in its ability to acquire resistance to any antibiotic (Chambers and DeLeo, 2009). In the present study, 33.3% of S. agalactiae were classified as penicillin-resistant. Our findings are similar to the results of the previous study with 57.1% antimicrobial resistance against S. agalactiae for penicillin (Najeeb et al., 2013). In this study, chloramphenicol, gentamicin, imipenem, norfloxacin and meropenem were found to be the most effective antimicrobials against E. coli isolates, confirming the data of Rudra and Dutta (2018). Vasquez-Garcia et al. (2017) reported that gentamicin was a less effective antimicrobial (50%) for E. coli isolates. In another study by Aydin et al. (2009) reported 100% resistance of E. coli isolates to norfloxacin which is in contrast with findings of the present study.

 

CONCLUSIONS

 

In conclusion, S. aureus was the most prevalent organisms in caprine mastitis followed by S. agalactiae and E. coli in the study area.The presence of S. aureus, S. agalactiae and E. coli from milk samples of both clinical and subclinical mastitis goats poses a threat to public health and dairy industry. Routine inspection with CMT is imperative in the diagnosis of mastitis, and bacterial isolation and antibiotic susceptibility testing are essential to control the disease and achieve effective treatment.

 

ACKNOWLEDGeMENTs

 

The authors thank the Research Acculturation Grant Scheme (RAGS) (Project code: RAGS/1/2015/SG0/UNISZA/02/2) for funding this study.

 

CONFLICT OF INTEREST

 

None of the authors have any potential conflict of interest to declare.

 

authors contribution

 

All authors contributed equally.

 

REFERENCES

 

  • Abdalhamed AM, Zeedan GMS, Abou Zeina HAA (2018). Isolation and identification of bacteria causing mastitis in small ruminants and their susceptibility to antibiotics, honey, essential oils, and plant extracts.Vet. World. 11(3): 355–362. https://doi.org/10.14202/vetworld.2018.355-362
  • Ali Z, Muhammad G, Ahmad T, Khan R, Naz S, Anwar H, Farooqi FA, Manzoor MN, Usama AR (2010). Prevalence of caprine sub-clinical mastitis, its etiological agents andtheir sensitivity to antibiotics in indigenous breeds of Kohat. Pak. J. Life Soc. Sci. 8(1): 63-67.
  • Aydin I, Kav K, Celik HA (2009). Identification and antimicrobial susceptibility of subclinical mastitis pathogens isolated from Hair Goats’ milk. J. Anim.Vet. Adv. 8(6): 1086-1090.
  • Barkema HW, Green MJ, Bradley AJ, Zadoks RN (2009). The role of contagious disease in udder health. J Dairy Sci. 92(10): 4717-4729. https://doi.org/10.3168/jds.2009-2347
  • Chambers HF, DeLeo FR (2009). Waves of resistance: Staphylococcus aureus in the antibiotic era. Nat. Rev. Microbiol. 7(9): 629-641. https://doi.org/10.1038/nrmicro2200
  • Contreras A, Sierra D, Sanchez A, Corrales JC, Marco JC, Paape MJ, Gonzalo C (2007). Mastitis in small ruminants. Small Rumin. Res. 68: 145-153. https://doi.org/10.1016/j.smallrumres.2006.09.011
  • Dasohari A, Kandula S (2017). Mastitis in goats - diagnosis and management. Int. J. Pure App. Biosci. 5(6): 448-451. https://doi.org/10.18782/2320-7051.5040
  • Ebrahimi A, Lotfalian, S, Karimi S (2007). Drug resistance in isolated bacteria from milk of sheep and goats with subclinical mastitis in Shahrekord district. Iranian J. Vet. Res. 8(1): 76-79.
  • Faiq TA, Ghazali MF, Chai MH, Ariffin SMZ (2017). Isolation of Staphylococcus aureus: clinical and subclinical mastitis infections in sheep and dairy goats. In: Proceedings of the 29th Veterinary Association Malaysia Congress (Shah Alam, Malaysia,Veterinary Association Malaysia), 60.
  • Hameed KGA, Sender G, Kossakowska AK (2007). Public health hazard due to mastitis in dairy cows. Anim. Sci. Pap. Rep. 26(2): 73-85.
  • Hawari AD, Obeidat M, Awaisheh SS, Al-Daghistani HI, Al-Abbadin AA, Omar SS, El-Qudah J (2014). Prevalence of mastitis pathogens and their resistance against antimicrobial agents in Awassi sheep in Al-Balqa province of Jordan. Am. J. Anim. Vet. Sci. 9(2): 116-121. https://doi.org/10.3844/ajavsp.2014.116.121
  • Hinthong W, Pumipuntu N, Santajit S, Kulpeanprasit S, Buranasinsup S, Sookrung N, Chaicumpa W, Aiumurai P, Indrawattana N (2017). Detection and drug resistance profile of Escherichia coli from subclinical mastitis cows and water supply in dairy farms in Saraburi Province, Thailand. Peer J. 5: e3431. https://doi.org/10.7717/peerj.3431
  • Jeph NK (2012). Clinico-therapeutic studies on clinical mastitis in Goats (Capra hircus), Master of Veterinary Science, Rajasthan University of Veterinary and Animal Sciences, Bikaner, India.
  • Landfried LK, Barnidge EK, Pithua P, Lewis RD, Jacoby JA, King CC, Baskin CR (2018). Antibiotic use on goat farms: an investigation of knowledge, attitudes, and behaviors of Missouri goat farmers. Animals (Basel). 8(11): 198. https://doi.org/10.3390/ani8110198
  • Lucia M, Rahayu S, Haerah D, Wahyuni D (2017). Detection of Staphylococcus aureus and Streptococcus agalactiae: subclinical mastitis causes in dairy cow and dairy buffalo (Bubalus Bubalis). Am. J. Biomed. Res. 5: 8-13.
  • Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, Harbarth S, Hindler JF, Kahlmeter G, Olsson-Liljequist B, Paterson DL, Rice LB, Stelling J, Struelens MJ, Vatopoulos A, Weber JT, Monnet DL (2012). Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin. Microbiol. Infect. 18(3):268-281. https://doi.org/10.1111/j.1469-0691.2011.03570.x
  • Najeeb MF, Anjum AA, Ahmad MUD, Khan HM, Ali MA, Sattar MMK (2013). Bacterial etiology of subclinical mastitis in dairy goats and multiple drug resistance of the isolates. J. Anim. Plant Sci. 23(6): 1541-1544.
  • Parra SA, Rather MI, Para PA, Ganguly S (2017). The emergence of drug resistant bacteria: effects on human health. J. Environ. Life Sci. 2 (3): 77-79.
  • Pirzada M, Malhi KK, Memon MI, Leghari RA, Abro1 SH, Leghari A, Habib F, Baloch H, Rahmatullah R (2016). In vitro antimicrobial susceptibility profile of sub-clinical mastitis isolates from dairy goats. J. Anim. Health Prod. 4(3): 72-77. https://doi.org/10.14737/journal.jahp/2016/4.3.72.77
  • Quinn P, Bryan M, Carter M, Carter GR (2004). Clinical Veterinary Microbiology, Mosby Publishing, St Louis, United States: 43-55: 327-344.
  • Rahman B, Ownagh A, Mardani K, Ardebili FF (2016). Prevalence and molecular characterization of Staphylococci isolated from sheep with subclinical mastitis in West-Azerbaijan province, Iran. Vet. Res. Forum. 7(2): 155-162.
  • Rainard P, Foucras G, Fitzgerald JR,Watts JL, Koop G, Middleton JR (2018). Knowledge gaps and research priorities in Staphylococcus aureus mastitis control. Transbound Emerg. Dis. 65(1):149–165. https://doi.org/10.1111/tbed.12698
  • Rinaldi M, Li RW, Capuco AV (2010). Mastitis associated transcriptomic disruptions in cattle. Vet. Immunol. Immunopathol. 138(4): 267-279. https://doi.org/10.1016/j.vetimm.2010.10.005
  • Rudra PG, Dutta A (2018). E. coli coliform mastitis in doe and its antibiogram. J. Bacteriol. Mycol. 5(1): 1059.
  • Sarker H, Samad MA (2011). Udder-halve-wise comparative prevalence of clinical and subclinical mastitis in lactating goats with their bacterial pathogens and antibiotic sensitivity patterns in Bangladesh. Bangl. J. Vet. Med. 9(2): 137-143. https://doi.org/10.3329/bjvm.v11i2.19138
  • Seegers H, Fourichon C, Beaudeau F (2003). Production effects related to mastitis and mastitis economics in dairy cattle herds.Vet. Res. 34(5): 475-491. https://doi.org/10.1051/vetres:2003027
  • Seyoum B, Kefyalew H, Abera B, Abdela N (2018). Prevalence, risk factors and antimicrobial susceptibility test of Staphylococcus aureus in bovine cross breed mastitic milk in and around Asella Town, Oromia Regional State, Southern Ethiopia. Acta Trop. 177: 32-36. https://doi.org/10.1016/j.actatropica.2017.09.012
  • Shamila-Syuhada AK, Rusul G, Wan-Nadiah WA, Chuah LO (2016). Prevalence and antibiotics resistance of Staphylococcus aureus isolates isolated from raw milk obtained from small-scale dairy farms in Penang, Malaysia. Pakistan Vet. J. 36(1): 98-102.
  • Tomazi T, Souza Filho AFD, Heinemann MB, Santos MVD (2018). Molecular characterization and antimicrobial susceptibility pattern of Streptococcus agalactiae isolated from clinical mastitis in dairy cattle Santos. PLoS ONE 13(6): e0199561. https://doi.org/10.1371/journal.pone.0199561
  • Vasquez-Garcia A, Silva TS, Queiroz SRA, Godoy SHH, Fernandes AZ, Sousa RLM, Franzolin R (2017). Species identification and antimicrobial susceptibility profile of bacteria causing subclinical mastitis in buffalo. Pesq. Vet. Bras. 37(5): 447-452. https://doi.org/10.1590/s0100-736x2017000500004
  • Wakwoya A, Molla B, Belihu K, Kleer J, Hildebrantdt G (2006). A cross-sectional study on the prevalence, antimicrobial susceptibility patterns and associated bacterial pathogens of goat mastitis. Int. J. Appl. Res. Vet. Med. 4(2): 169-176.
  • Wegener HC (2012). Antibiotic resistance-linking human and animal health. In: Institute of Medicine (US). Improving Food Safety Through a One Health Approach: Workshop Summary, National Academies Press, Washington, USA, A15.
  • White EC, Hinckley LS (1999). Prevalence of mastitis pathogens in goat milk. Small Rum. Res. 33(2):117-121. https://doi.org/10.1016/S0921-4488(99)00013-9
  • Zhao Y, Liu H, Zhao X, Gao Y, Zhang M, Chen D (2015). Prevalence and pathogens of subclinical mastitis in dairy goats in China.Trop. Anim. Health Prod. 47(2):429-435. https://doi.org/10.1007/s11250-014-0742-y
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